**Title:** Interpreting Proton NMR Spectroscopy Data **Objective:** Draw the structure of the compound based on the given spectroscopy data. **Compound Formula:** C₆H₁₂O **Proton NMR Spectroscopy Data:** - **2.6 ppm, 1H, sextet:** - Indicates a proton with six neighboring equivalent protons. - **2.1 ppm, 3H, singlet:** - Represents three equivalent protons with no neighboring proton interactions. - **1.7 – 1.3 ppm, 2H, multiplet:** - Two protons experiencing complex splitting due to multiple different neighboring protons. - **1.1 ppm, 3H, doublet:** - Three equivalent protons split by one adjacent proton. - **0.9 ppm, 3H, triplet:** - Three equivalent protons split by two neighboring protons. **Assignment:** Using the provided NMR data, deduce and sketch the molecular structure of the compound C₆H₁₂O. Consider the integration values and splitting patterns to make accurate connections between the atoms. **Note:** Proton NMR spectroscopy helps elucidate the structure by showing how different hydrogen atoms in a molecule experience the magnetic environment differently, leading to the splitting patterns observed.

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
ChapterL4: Proton (1h) Nmr Spectroscopy
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**Title:** Interpreting Proton NMR Spectroscopy Data

**Objective:** Draw the structure of the compound based on the given spectroscopy data.

**Compound Formula:** C₆H₁₂O

**Proton NMR Spectroscopy Data:**

- **2.6 ppm, 1H, sextet:**
  - Indicates a proton with six neighboring equivalent protons.
  
- **2.1 ppm, 3H, singlet:**
  - Represents three equivalent protons with no neighboring proton interactions.

- **1.7 – 1.3 ppm, 2H, multiplet:**
  - Two protons experiencing complex splitting due to multiple different neighboring protons.

- **1.1 ppm, 3H, doublet:**
  - Three equivalent protons split by one adjacent proton.

- **0.9 ppm, 3H, triplet:**
  - Three equivalent protons split by two neighboring protons.

**Assignment:**
Using the provided NMR data, deduce and sketch the molecular structure of the compound C₆H₁₂O. Consider the integration values and splitting patterns to make accurate connections between the atoms.

**Note:** Proton NMR spectroscopy helps elucidate the structure by showing how different hydrogen atoms in a molecule experience the magnetic environment differently, leading to the splitting patterns observed.
Transcribed Image Text:**Title:** Interpreting Proton NMR Spectroscopy Data **Objective:** Draw the structure of the compound based on the given spectroscopy data. **Compound Formula:** C₆H₁₂O **Proton NMR Spectroscopy Data:** - **2.6 ppm, 1H, sextet:** - Indicates a proton with six neighboring equivalent protons. - **2.1 ppm, 3H, singlet:** - Represents three equivalent protons with no neighboring proton interactions. - **1.7 – 1.3 ppm, 2H, multiplet:** - Two protons experiencing complex splitting due to multiple different neighboring protons. - **1.1 ppm, 3H, doublet:** - Three equivalent protons split by one adjacent proton. - **0.9 ppm, 3H, triplet:** - Three equivalent protons split by two neighboring protons. **Assignment:** Using the provided NMR data, deduce and sketch the molecular structure of the compound C₆H₁₂O. Consider the integration values and splitting patterns to make accurate connections between the atoms. **Note:** Proton NMR spectroscopy helps elucidate the structure by showing how different hydrogen atoms in a molecule experience the magnetic environment differently, leading to the splitting patterns observed.
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